Zobrazeno 1 - 10
of 312
pro vyhledávání: '"Meryem B"'
Autor:
Meryem B. Baghdadi, Tae-Hee Kim
Publikováno v:
STAR Protocols, Vol 3, Iss 2, Pp 101351- (2022)
Summary: This protocol describes the isolation and culture of 3D intestinal crypt organoids with stromal niche cells. We show a murine organoid culture system that utilizes conditioned media isolated from primary, mucosal enteric glial cell culture.
Externí odkaz:
https://doaj.org/article/cce1b26b9e264dc78c4d0eceb3315a96
Autor:
Natalia Pietrosemoli, Sébastien Mella, Siham Yennek, Meryem B. Baghdadi, Hiroshi Sakai, Ramkumar Sambasivan, Francesca Pala, Daniela Di Girolamo, Shahragim Tajbakhsh
Publikováno v:
Skeletal Muscle, Vol 7, Iss 1, Pp 1-15 (2017)
Abstract Background Skeletal muscle satellite (stem) cells are quiescent in adult mice and can undergo multiple rounds of proliferation and self-renewal following muscle injury. Several labs have profiled transcripts of myogenic cells during the deve
Externí odkaz:
https://doaj.org/article/efc5e7c8864448cf80616e560368d16f
Autor:
Natalia Pietrosemoli, Sébastien Mella, Siham Yennek, Meryem B. Baghdadi, Hiroshi Sakai, Ramkumar Sambasivan, Francesca Pala, Daniela Di Girolamo, Shahragim Tajbakhsh
Publikováno v:
Skeletal Muscle, Vol 8, Iss 1, Pp 1-1 (2018)
After publication of this article [1], the authors noted that the legends for supplementary files Figures S3 and S4 were truncated in the production process, therefore lacking some information concerning these Figures. The complete legends are includ
Externí odkaz:
https://doaj.org/article/5a57a95f0fbb4698911fca857eb448f7
Autor:
Meryem B. Baghdadi, Tae-Hee Kim
Publikováno v:
Seminars in Cell & Developmental Biology. :43-49
Akademický článek
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Autor:
Idil Karaca Acari, Fatma Kurul, Meryem Beyza Avci, S. Deniz Yasar, Seda Nur Topkaya, Ceyhun Açarı, Erbil Ünsal, Balahan Makay, Süleyman Köytepe, Burhan Ateş, İsmet Yilmaz, Turgay Seçkin, Arif E. Cetin
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-17 (2024)
Abstract Familial Mediterranean Fever (FMF) is an autosomal recessive genetic disorder, primarily observed in populations around the Mediterranean Sea, linked to MEFV gene mutations. These mutations disrupt inflammatory responses, increasing pyrin-pr
Externí odkaz:
https://doaj.org/article/031608cda770471f8158d7b4047dac50
Publikováno v:
Journal of Ecological Engineering, Vol 25, Iss 10, Pp 176-188 (2024)
This work aimed to study the seasonal impact on the pollutant removal efficiency of constructed wetland (CW) units that treat domestic wastewater in the region of Rabat, Morocco. In this context, four vertical flow-constructed wetlands (VFCWs) were i
Externí odkaz:
https://doaj.org/article/196647147c944a9ebc099b40c6dbc2b7
Autor:
Rajae Ghibate, Meryem Ben Baaziz, Mohammed Chrachmy, Meryem Kerrou, Rachid Taouil, Omar Senhaji
Publikováno v:
Ecological Engineering & Environmental Technology, Vol 25, Iss 10, Pp 96-106 (2024)
This study explores the production of activated carbon from agricultural waste, specifically Punica granatum peel, and its application as an eco-friendly solution for removing Cu2+ ions from industrial effluents, particularly from copper-plating indu
Externí odkaz:
https://doaj.org/article/fe0a748f24a84ad0bb2e2b9a3aae03c9
Autor:
Fatima Saddouki, MD, Fatima Oussi, MD, Insaf Rhalem, MD, Nizar El Bouardi, MD, Amal Akammar, MD, Meryem Haloua, MD, My Youssef Alaoui Lamrani, MD, Meryem Boubbou, MD, Mustapha Maaroufi, MD, Badr Alami, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 10, Pp 4631-4635 (2024)
Pilonidal sinus disease is a frequent and recurrent pathology in young adults, with a male predominance, while malignant transformation of the pilonidal sinus is a rare complication, it occurs in 0.1% of patients, with a poor prognosis. Early surgica
Externí odkaz:
https://doaj.org/article/a5df6165e5884274a532b7ed56c74b48
Autor:
Hanaa El Ghiati, MD, Abdelilah Benelmakki, MD, Jihane Fagouri, MD, Jaouad Nguadi, MD, Meryem Bennani, MD, Jamal Kheyi, MD, Hicham Bouzelmat, MD, Aatif Benyass, MD, Ali Chaib, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 10, Pp 4293-4296 (2024)
Cleidocranial dysplasia (CCD) is a rare genetic disorder characterized by skeletal abnormalities, including hypoplastic or absent clavicles, delayed closure of cranial sutures, and dental anomalies.We present a case of a 72-year-old female with a his
Externí odkaz:
https://doaj.org/article/0f61c0b04251426ea334192ed24076ea